Amanda Fosang

Last updated
Amanda Fosang

AM
Born
Nationality Australia
Scientific career
FieldsArthritis, cartilage, skeletal development, metalloproteinases, aggrecan
Institutions The University of Melbourne and Murdoch Children's Research Institute

Amanda Jane Fosang AM is a biomedical researcher who has pioneered arthritis research in Australia.

Contents

Career

Fosang is a Principal Research Fellow with the National Health and Medical Research Council (NHMRC) of Australia who has an established career researching arthritis and cartilage biology in health and disease. [1] She is Professor and Group Leader of Arthritis Research at the Murdoch Childrens Research Institute (MCRI) and the University of Melbourne Department of Paediatrics. Fosang returned to Australia after completing her post-doctoral studies at the Kennedy Institute of Rheumatology in London, [1] and was awarded an RD Wright Fellowship by the NHMRC in 1994. Since then she has received continuous competitive grant and fellowship funding from the NHMRC. [2] She joined the University of Melbourne, Department of Medicine in 1990, and moved to the Department of Paediatrics in 1994. Fosang became a Group Leader of the MCRI at its inception in 2000.

Research Program

The goal of Fosang's research program is to understand the complex interactions between cartilage cells and their matrix, in both healthy cartilage and arthritic diseases. Her work focuses on the structure and function of the cartilage molecules, aggrecan and type II collagen, and the enzymes that destroy them in arthritic disease. She and her team have generated unique mice for evaluating cartilage damage in arthritic disease. Her work showing that ADAMTS-5 is the major aggrecanase in mouse cartilage was published in the high-profile international journal Nature in 2005. [3]

More recently, Fosang's group has been studying the degradation products generated by these enzymes, and how these products might regulate cellular function. Some studies are done in explant and cell culture systems, or with highly purified enzymes and substrates in vitro. Other studies use unique, genetically modified mice that have been engineered to resist cartilage destruction. Studies with these mice can provide valuable insights into the mechanisms of joint remodelling in development and disease. Her studies on cartilage biology and arthritic diseases will identify new target molecules and/or activities, for the development of disease-modifying arthritis therapies. [4]

Professional Service

Fosang joined the Board of Directors for the Osteoarthritis Research Society International (OARSI) in 2012 and was appointed Chair of the OARSI Asian Task Force in 2013. She is the first Australian appointed to the Journal of Biological Chemistry as an Associate Editor. [1] An educator and mentor of upcoming scientists, Fosang coordinates the Bachelor of Science (BSc) and Bachelor of Biomedicine (BBMed) Honours Program for the University of Melbourne (Department of Paediatrics) and the MCRI. [1] She has also supervised five PhD students and eleven BSc Honours students to course completion. [2]

Awards

Related Research Articles

Arthritis type of joint disorder

Arthritis is a term often used to mean any disorder that affects joints. Symptoms generally include joint pain and stiffness. Other symptoms may include redness, warmth, swelling, and decreased range of motion of the affected joints. In some types of arthritis, other organs are also affected. Onset can be gradual or sudden.

Rheumatology is a branch of medicine devoted to the diagnosis and therapy of rheumatic diseases. Physicians who have undergone formal training in rheumatology are called rheumatologists. Rheumatologists deal mainly with immune-mediated disorders of the musculoskeletal system, soft tissues, autoimmune diseases, vasculitides, and inherited connective tissue disorders.

Osteoarthritis Form of arthritis caused by degeneration of joints

Osteoarthritis (OA) is a type of degenerative joint disease that results from breakdown of joint cartilage and underlying bone. The most common symptoms are joint pain and stiffness. Usually the symptoms progress slowly over years. Initially they may occur only after exercise but can become constant over time. Other symptoms may include joint swelling, decreased range of motion, and, when the back is affected, weakness or numbness of the arms and legs. The most commonly involved joints are the two near the ends of the fingers and the joint at the base of the thumbs; the knee and hip joints; and the joints of the neck and lower back. Joints on one side of the body are often more affected than those on the other. The symptoms can interfere with work and normal daily activities. Unlike some other types of arthritis, only the joints, not internal organs, are affected.

The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) is one of the institutes and centers that make up the National Institutes of Health, an agency of the United States Department of Health and Human Services (HHS).

Glucosamine (C6H13NO5) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. Glucosamine is part of the structure of two polysaccharides, chitosan and chitin. Glucosamine is one of the most abundant monosaccharides. Produced commercially by the hydrolysis of shellfish exoskeletons or, less commonly, by fermentation of a grain such as corn or wheat, glucosamine has many names depending on country.

ADAMTS5

A disintegrin and metalloproteinase with thrombospondin motifs 5 also known as ADAMTS5 is an enzyme that in humans is encoded by the ADAMTS5 gene.

Barbara Ansell

Barbara Mary Ansell, CBE, FRCP, FRCS was the founder of paediatric rheumatology. Ansell was notable for outstanding contributions to the advancement of paediatric knowledge, specifically defining chronic joint disorders and the improvement of their management.

Aggrecan

Aggrecan (ACAN), also known as cartilage-specific proteoglycan core protein (CSPCP) or chondroitin sulfate proteoglycan 1, is a protein that in humans is encoded by the ACAN gene. This gene is a member of the lectican family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage.

Aggrecanases are extracellular proteolytic enzymes that are members of the ADAMTS family. Aggrecanases act on large proteoglycans known as aggrecans, which are components of connective tissues such as cartilage. The inappropriate activity of aggrecanase is a mechanism by which cartilage degradation occurs in diseases such as arthritis. At least two forms of aggrecanase exist in humans: ADAMTS4 or aggrecanase-1 and ADAMTS5 or aggrecanase-2. Both proteins contain thrombospondin (TS) motifs required for proper recognition of substrates. Although both proteins can cleave the substrate aggrecan at the same position, they differ in kinetics and in secondary cleavage sites.

ADAMTS4

A disintegrin and metalloproteinase with thrombospondin motifs 4 is an enzyme that in humans is encoded by the ADAMTS4 gene.

MMP19

Matrix metalloproteinase-19 (MMP-19) also known as matrix metalloproteinase RASI is an enzyme that in humans is encoded by the MMP19 gene.

Gene therapy is being studied as a treatment for osteoarthritis (OA). Unlike pharmacological treatments which are administered systemically, gene therapy aims to establish sustained, synthesis of gene products and tissue rehabilitation within the joint.

There is a history of clinical research done on glycosaminoglycans, especially glucosamine and chondroitin, for the treatment of arthritis. Since glucosamine is a precursor for glycosaminoglycans, and glycosaminoglycans are major components of cartilage, ingesting glucosamine might nourish joints, and thereby alleviate arthritis symptoms.

A disintegrin and metalloproteinase with thrombospondin motifs 7 (ADAMTS7) is an enzyme that in humans is encoded by the ADAMTS7 gene on chromosome 15. It is ubiquitously expressed in many tissues and cell types. This enzyme catalyzes the degradation of cartilage oligomeric matrix protein (COMP) degradation. ADAMTS7 has been associated with cancer and arthritis in multiple tissue types. The ADAMTS7 gene also contains one of 27 SNPs associated with increased risk of coronary artery disease.

Melissa Little Australian scientist and academic (born 1963)

Professor Melissa Little is an Australian scientist and academic, currently Theme Director of Cell Biology, heading up the Kidney Research laboratory at the Murdoch Children's Research Institute. She is also a Professor in the Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, and Program Leader of Stem Cells Australia.

Post-traumatic arthritis Medical condition

Post-traumatic arthritis (PTA) is a form of osteoarthritis following an injury to a joint.

Katrina Jane Allen is an Australian politician and former medical researcher who has been a member of the House of Representatives since the 2019 federal election. She is a member of the Liberal Party and represents the Division of Higgins in Victoria.

A disease-modifying osteoarthritis drug (DMOAD) is a drug that would inhibit or even reverse the progression of osteoarthritis. Since the main hallmark of osteoarthritis is cartilage loss, a typical DMOAD would prevent the loss of cartilage and potentially regenerate it. Other DMOADs may attempt to help repair adjacent tissues by reducing inflammation. A successful DMOAD would be expected to show an improvement in patient pain and function with an improvement of the health of the joint tissues.

Vera Ignjatovic is an Australian haematologist and former handball player.

Rachelle Buchbinder Australian rheumatologist and medical researcher

Rachelle Buchbinder is an Australian rheumatologist and clinical epidemiologist. Her clinical practice is in conjunction with research involving multidisciplinary projects relating to arthritis and musculoskeletal conditions. She promotes improvement of communication with patients and health literacy in the community.

References

  1. 1 2 3 4 5 6 7 Mukhopadhyay, Rajendrani (February 2014). "Meet Amanda Fosang: A new associate editor of The Journal of Biological Chemistry". ASBMB Today. Archived from the original on 14 August 2014. Retrieved 15 August 2014.CS1 maint: discouraged parameter (link)
  2. 1 2 "A/Professor Amanda Fosang". Murdoch Childrens Research Institute. Archived from the original on 14 August 2014. Retrieved 15 August 2014.CS1 maint: discouraged parameter (link)
  3. Stanton H, Rogerson FM, East CJ, Golub SB, Lawlor KE, Meeker CT, Little CB, Last K, Farmer PJ, Campbell IK, Fourie AM, Fosang AJ. ADAMTS5 is the major aggrecanase in mouse cartilage in vivo and in vitro. Nature. 2005 Mar 31;434(7033):648-52.
  4. Fosang, Amanda J., and Christopher B. Little. "Drug insight: aggrecanases as therapeutic targets for osteoarthritis." Nature Clinical Practice Rheumatology 4.8 (2008): 420-427.
  5. "Professor Amanda Jane FOSANG". It's An Honour. Retrieved 2021-01-26.